Stéphanie Delstanche
-
- Neurogenetic and Muscular Disorders Research 4
-
- Transcranial Magnetic Stimulation Studies 2
- Amyotrophic Lateral Sclerosis Research 2
-
- Glycogen Storage Diseases and Myoclonus 1
-
- Congenital Anomalies and Fetal Surgery 2
-
- Protein Kinase Regulation and GTPase Signaling 2
- RNA modifications and cancer 2
- Amyloidosis: Diagnosis, Treatment, Outcomes 2
- Co-authors
- Jean SchoenenShahram AttarianJuan F. Vázquez‐CostaValeria SansoneMaggie C. WalterHanns LochmüllerGauthier RemicheJan De Bleecker
- Partner nations
- BelgiumFranceUnited Kingdom
In The Last Decade
Stéphanie Delstanche
11 papers receiving 140 citations
Peers
Comparison fields: 5 of 39
- Genetics 59
- Neurology 32
- Obstetrics and Gynecology 9
- Cellular and Molecular Neuroscience 20
- Rheumatology 16
Countries citing papers authored by Stéphanie Delstanche
This map shows the geographic impact of Stéphanie Delstanche's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Stéphanie Delstanche with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stéphanie Delstanche more than expected).
Fields of papers citing papers by Stéphanie Delstanche
This network shows the impact of papers produced by Stéphanie Delstanche. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Stéphanie Delstanche. The network helps show where Stéphanie Delstanche may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Stéphanie Delstanche, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 10 | |
| 2 | 2024 | 0 | |
| 3 | 2024 | 0 | |
| 4 | 2023 | 6 | |
| 5 | 2023 | 11 | |
| 6 | 2022 | 6 | |
| 7 | 2021 | 8 | |
| 8 | 2020 | 27 | |
| 9 | 2020 | 38 | |
| 10 | [Infantile spinal muscular atrophy : therapeutic (R)evolution]. | 2019 | 1 |
| 11 | 2017 | 2 | |
| 12 | 2010 | 29 | |
| 13 | Botulinum toxin for the treatment of headache: a promising path on a "dead end road"? | 2010 | 5 |
About Stéphanie Delstanche
Stéphanie Delstanche is a scholar working on Genetics, Neurology and Neurology, having authored 13 papers that have together received 143 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (4 papers), Transcranial Magnetic Stimulation Studies (2 papers), Congenital Anomalies and Fetal Surgery (2 papers), Amyotrophic Lateral Sclerosis Research (2 papers), Protein Kinase Regulation and GTPase Signaling (2 papers), RNA modifications and cancer (2 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (2 papers) and Glycogen Storage Diseases and Myoclonus (1 paper). The work is most often cited by research in Genetics (59 citations), Neurology (32 citations) and Obstetrics and Gynecology (9 citations). Stéphanie Delstanche has collaborated with scholars based in Belgium, France and United Kingdom. Frequent co-authors include Jean Schoenen, Shahram Attarian, Juan F. Vázquez‐Costa, Valeria Sansone, Maggie C. Walter, Hanns Lochmüller, Gauthier Remiche, Jan De Bleecker, Kristl G. Claeys and Eugenio Mercuri. Their work appears in journals such as Neurology, Glia and Clinical Neurophysiology.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.